FdaApplication
NDA 017661
Identifiers
- fda_app_no: NDA017661
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1992-08-21 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TAVIST | CLEMASTINE FUMARATE | 2.68MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| TAVIST-1 | CLEMASTINE FUMARATE | 1.34MG | TABLET;ORAL |
| TAVIST-1 | CLEMASTINE FUMARATE | 1.34MG | TABLET;ORAL |
3 products